Phenotypes for disease #01942 (holocarboxylase synthetase deficiency, OMIM:253270)

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AscendingPhenotype ID     

Phenotype details     

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Individual ID     
0000340196 Micropenis, unilateral chryptorchidism, few gluteal cafe-au-lait spot, developmental regression, autistic behavior Holocarboxylase synthetase deficiency Holocarboxylase synthetase deficiency Familial, autosomal recessive - 08y01m - - - Miriam Erandi Reyna-Fabián 00451459
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